Pulmonary Arterial Hypertension
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Transcript Pulmonary Arterial Hypertension
Definition
Increased blood pressure in the pulmonary artery, veins,
or capillaries
Progressive disease leading to Right ventricular failure
and eventual death
Right Heart Catheterization Findings
Mean Pulmonary Arterial Pressure ≥ 25
Pulmonary Capillary Wedge Pressure ≤ 15
Pulmonary Vascular Resistance > 3 wood units (this part not
included in definition)
Pathophysiology
Disease Pathways
Classification of Causes
Group 1
Idiopathic & Heritable
Autoimmune disease/ Connective Tissue disease
HIV
Drugs and toxins
Portal Hypertension
Congenital Heart Disease
Schistosomiasis
Group 2 (Left heart disease)
Group 3 (lung disease)
COPD
Interstitial Lung disease
OSA
Group 4
Chronic Thromboembolic Disease (chronic pulmonary emboli)
Group 5 (Miscellaneous)
WHO Group 1 PAH
Epidemiology (1)
Patient Population
• Prevalence
• 12 of every 1
million
Americans
• Incidence
• Approximately 2
new cases per
million are
diagnosed yearly
in US
• Primarily Female (78%)
(1)
• Mean age at diagnosis is
47 years (1)
• Mean time from first
symptoms to diagnosis
of 31 months (2)
Common Risk
Factors
• Family History
• Genetic Mutations
(BMPR2)
• HIV
• Connective Tissue
Disease
• Anorexigen use
• Portal Hypertension
• Illicit Drug Use
• Congenital Heart
Disease
Who Group 1 Subtypes (REVEAL
Registry)
Other
0.5%
Familial PAH
3%
Idiopathic PAH
46%
Badesh DB, et al. Chest 2010; 137(2):376-387
Associated PAH
51%
Associated PAH Etiologies
Congenital Heart
Disease
19%
Other
5%
CVD/CTD
50%
HIV
4%
Portal HTN
11%
Drugs/ Toxins
11%
Badesh DB, et al. Chest 2010; 137(2):376-387
Symptoms
Dyspnea
Fatigue
Exertional intolerance
Chest Pain (late)
Syncope/ Dizziness (late)
Palpitations
Abdominal Distention
Physical Findings
Peripheral Edema
Ascites
Loud P2
Pansystolic Murmur
* Lung sounds often normal
NYHA Functional Class
Diagnosis
Right heart catheterization is required to
accurately diagnose PAH
Echocardiogram is used as screening tool and to
monitor treatment efficacy
Diagnosis Cont’d
Extensive work-up completed to evaluate for all possible
underlying causes
PFTS, CT of Chest to r/o lung disease
VQ scan to r/o chronic PE
Blood serologies to check for autoimmune disease & HIV
Nocturnal Polysomnogram (if patient has symptoms of
sleep apnea)
Echocardiogram
(Apical 4- chamber view)
Normal
PAH
Treatment
Modalities targeting 3 separate pathways
Treatment Cont’d
Phosphodiesterase Type 5 Inhibitors (PDE5 Inhibitors)
Revatio (Sildenafil)- oral
Adcirca (Tadalafil) - oral
Endothelin Receptor Antagonists (ERAs)
Letairis (Ambrisentan)- oral
Opsumit (Macitentan) - oral
Tracleer (Bosentan)- oral (rarely used anymore)
Prostacyclins
Oral
Orenitram (Treprostinil)
Uptravi (Selexipag)
Inhaled
Tyvaso (Treprostinil)
Ventavis (Iloprost)
IV
Remodulin (Treprostinil) – also available in SC (subcutaneous) form
Veletri (epoprostenol)
Flolan (epoprostenol)
Treatment Cont’d
Soluble Guanylate Cyclase stimulator
Adempas (Riociquat)
Monitoring
Echocardiogram
6 minute walk test
Laboratory data
Repeat RHC if not clinically improved or declining
Role of Pulmonary Rehab in PAH
Research studies show that pulmonary rehab increases
6MWT distance and increases peak Vo2
Gives patients ability to network with other patients
like them
Aids in weight loss for some
Case Study
57 yr old AA female
Comorbidities: Scleroderma
Diagnosed with PAH April 2014 by RHC
Symptoms
Fatigue
Dyspnea
Peripheral edema
Diagnostics
CT of Chest with minimal scarring left base, small pericardial effusion
VQ low probability PE
Autoimmune serologies negative except highly positive ANA
PFTS with Restrictive Lung disease
Case Study
Before Treatment
Echocardiogram - RVSP 80-85 mmHg, RVID 4.1 cm
RHC – PA Mean 53, PCWP 8, LVEDP 8, CO 2.3 liters
6MWT - 54 meters
Patient started on Adcirca & Letairis
Repeat Testing May 2014
Echo - RVSP 105-100 mmHg, RVID 3.3 cm, TAPSE 1.6 cm
RHC – PA Mean 50, PCWP 7, CO 3.1 liters
6MWT – 162 meters
Normal Values: RVID 0.8-2.6, TAPSE > 1.6
Case Study
IV Remodulin intitiated
Repeat Echo - RVSP 80-85 mmHg, RVID 2.8 cm, TAPSE 2.3
6MWT – 54 meters
Symptoms after IV Remodulin
Less peripheral edema
Dyspnea improved, but still present
Fatigue resolving
Normal Values: RVID 0.8-2.6, TAPSE > 1.6
What is important for you to
know??
All PAH medications come from a specialty pharmacy and
are shipped to the patient’s home
They are VERY expensive
The only PAH medications that are on Providence hospital
formulary are Remodulin % Veletri
All other meds (PO & inhaled) must be brought from
home
Inhaled medications are delivered using special nebulizer
machine that patient must bring from home
What is important for you to
know??
Patients with SC or IV Remodulin cannot have their
infusions disrupted
Nothing else can be given through a Remodulin dedicated
line
SC/IV pumps should be checked on admission and daily
with dose verified with pharmacy to ensure correct
infusion rates
There is always a number on the specialized home pump to
call for any questions on what the patient’s rate should be
Center for Excellence
Providence Hospital will be applying to become a Center
for Excellence for diagnosis and treatment of PAH in
January 2015
This designation will bring nationwide recognition
It is imperative that all our staff be familiar with the PAH
diagnosis and all treatment modalities